Stage-Specific Excitation of Cannabinoid Receptor Exhibits Differential Effects on Mouse Embryonic Development
Anandamide ( N -arachidonoylethanolamine), an arachidonic acid derivative, is an endogenous ligand for both the brain-type (CB1-R) and spleen-type (CB2-R) cannabinoid receptors. We have previously demonstrated that preimplantation mouse embryos express mRNA for these receptors and that the periimpla...
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Veröffentlicht in: | Biology of reproduction 1999-04, Vol.60 (4), p.839-844 |
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Zusammenfassung: | Anandamide ( N -arachidonoylethanolamine), an arachidonic acid derivative, is an endogenous ligand for both the brain-type (CB1-R) and spleen-type
(CB2-R) cannabinoid receptors. We have previously demonstrated that preimplantation mouse embryos express mRNA for these receptors
and that the periimplantation uterus contains the highest level of anandamide yet discovered in a mammalian tissue. We further
demonstrated that 2-cell mouse embryos exposed to low levels of anandamide (7 nM) or other known cannabinoid agonists in culture
exhibit markedly compromised embryonic development to blastocysts and that this effect is mediated by CB1-R. In contrast,
the present study demonstrates that blastocysts exposed in culture to the same low levels of cannabinoid agonists exhibited
accelerated trophoblast differentiation with respect to fibronectin-binding activity and trophoblast outgrowth. Again, these
effects resulted from activation of embryonic CB1-R. There was a differential concentration-dependent effect of cannabinoids
on the trophoblast, with an observed inhibition of differentiation at higher doses. These results provide evidence for the
first time that cannabinoid effects are differentially executed depending on the embryonic stage and cannabinoid levels in
the environment. Since uterine anandamide levels are lowest at the sites of implantation and highest at the interimplantation
sites, the new findings imply that site-specific levels of anandamide and/or other endogenous ligands in the uterus may regulate
implantation spatially by promoting trophoblast differentiation at the sites of blastocyst implantation. |
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ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod60.4.839 |